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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06201871
Other study ID # IANB
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 2, 2024
Est. completion date March 2, 2024

Study information

Verified date January 2024
Source Jamia Millia Islamia
Contact Vivek Aggarwal
Phone 9818188358
Email drvivekaggarwal@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This prospective, randomized, double-blind clinical trial will be carried out Conservative Dentistry, Faculty of Dentistry, Jamia Millia Islamia. Seventy adult patients (35 alcoholic and 35 non-alcoholics) with symptomatic irreversible pulpits in a mandibular first or second molar will receive an IANB with 2% lidocaine. In case of pain during treatment, the procedure will be stopped, and the patients will be asked to rate the pain on the Heft-Parker scale. The injection shall be considered as successful if the patient reports pain scores less than 55 on the HP scale.


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date March 2, 2024
Est. primary completion date March 2, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - Symptomatic carious exposed mandibular first or second molars. - Alcoholic patients: Patient with low-moderate drinking levels according to the US National Institute on Alcohol Abuse and Alcoholism - Control patients: No history of alcohol consumption - Positive and prolonged response to thermal sensitivity tests and electric pulp test. - Vital coronal pulp on access cavity preparation. - American Society of Anesthesiologists class I or II medical history. - Ability to understand the use of pain scales. Exclusion Criteria: - Active pain in more than 1 teeth - Teeth with fused roots. - Radiographic evidence of an extra root. - Large restorations with overhanging margins. - Full crowns or deep periodontal pockets. - Hypertension or cardiovascular diseases, compromised immunity, active infection or inflammation - Known allergy or contraindications to any content of the local anesthetic solution or non-steroidal anti-inflammatory drugs (NSAIDs) - History of known or suspected drug abuse. - Taking any drugs which could affect the pain perception, e.g, opioids, antidepressants, anticonvulsants, muscle relaxants, anxiolytics, sedatives, nsaids. 23 - Pregnant or breastfeeding patients. - Patients with asthma, gastric ulcers, bleeding disorders.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Lidocaine Hydrochloride
Patients will receive an inferior alveolar nerve block injection using 1.8 mL of 2% lidocaine with 1: 80 000 epinephrine using a direct Halsted approach.

Locations

Country Name City State
India Faculty of Dentistry, Jamia MIliia Islamia New Delhi

Sponsors (1)

Lead Sponsor Collaborator
Jamia Millia Islamia

Country where clinical trial is conducted

India, 

Outcome

Type Measure Description Time frame Safety issue
Primary Anesthetic success The injection shall be considered as successful if the patient reports pain scores less than 55 on the visual analouge scale. The scale is 170mm long, with 0 marked as no pain and 170 marked as the maximum pain. 15 minutes following the injection
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